HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398856Generated: October 30, 2026
p-Anisoyl chloride → methyl N-(4-methoxybenzoyl)phenylalanyltyrosinate
https://huagongshe.com/reaction/2398856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl phenylalanyltyrosinate hydrochloride | HCID 70615103 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | methyl N-(4-methoxybenzoyl)phenylalanyltyrosinate | HCID 53971131 | 82% |
Reaction Steps
In a mixture of 10 ml of water and 50 ml of chloroform were suspended 3.79 g of methyl phenylalanyltyrosinate hydrochloride and 0.53 g of sodium carbonate. To the mixture was added dropwise 1.75 g of 4-methoxybenzoylchloride in parallel with 10 ml of sodium carbonate solution (0.75 g), while stirring and cooling with ice. The mixture was stirred for 2 hours and the chloroform layer was collected. The layer was washed with 5% hydrochloric acid and water, dried and concentrated to dryness. The residue was crystallized from ethyl acetate to give 3.9 g of methyl N-(4-methoxybenzoyl)-phenylalanyltyrosinate with a mp. 195°-197° C. in a yield of 82%. Analysis, calculated for C27H28O6N2 : C, 68.05; H, 5.92; N, 5.88; found C, 68.42; H, 6.08; N, 5.74.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04025644 |
|---|
| Source dataset | uspto-grants-1977_05 |
|---|
| ORD ID | ord-e5a655e11623418baecdf8dab9c564ec |
|---|
| Source note | uspto-grants-1977_05 |
|---|